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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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117 records meeting your search criteria returned- Product Code: OPR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
SEQUENT MEDICAL, INC WEB LOW PROFILE SL-USA W4-4-3FOR US 02/03/2020
MICROVENTION, INC. WEB SL 12/07/2019
SEQUENT MEDICAL, INC WEB LOW PROFILE SL-USA W4-6-4FOR US 11/14/2019
SEQUENT MEDICAL, INC WEB LOW PROFILE SL-USA W4-6-5FOR US 09/19/2019
SEQUENT MEDICAL, INC WEB SL 21 SINGLE LAYER W4-4-3 08/30/2019
SEQUENT MEDICAL, INC WEB LOW PROFILE SL-USA W4-5-3FOR US 06/20/2019
SEQUENT MEDICAL, INC WEB LOW PROFILE SL-USA W4-4-3FOR US 06/14/2019
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